5-Hydroxytryptophan Chemical Identity
5-Hydroxytryptophan has the molecular formula C11H12N2O3 and the molecular weight 220.2. The structure is an indole ring carrying a hydroxyl group at position 5, joined through a methylene group to an alpha-amino acid. The natural, L-form has the (2S) configuration, and the CAS number 4350-09-8 belongs to it, while other numbers in circulation refer to the racemic or unspecified form. The molecule is a zwitterion in water, and its indole nucleus is electron-rich and sensitive to oxidation.
In biochemistry, 5-hydroxytryptophan is an intermediate on the biosynthetic route from tryptophan to serotonin, which is why the amino acid is well known beyond the plant itself. The natural source here is the seed of Griffonia simplicifolia (Vahl ex DC.) Baill., in which it occurs as a free amino acid at a high level together with lectins and sugars. The seed is also supplied as Griffonia Seed Extract Powder, a 10:1 ratio extract with no marker figure. That product describes the seed material, and the purified amino acid is a separate ingredient defined by the compound and its purity.
The single-compound identity matters for labeling. Tryptophan, 5-hydroxytryptophan and serotonin differ by one hydroxyl or by a decarboxylation, and a name that drops the hydroxy prefix describes a different molecule. Regulatory treatment of 5-hydroxytryptophan also differs between markets, so a buyer should check the intended market before use.












